A citation-based method for searching scientific literature

Klaus Hoeyer. Biotechnol Genet Eng Rev 2008
Times Cited: 53







List of co-cited articles
212 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
158
26



Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
16

Tissue donation to biobanks: a review of sociological studies.
Wendy Lipworth, Rowena Forsyth, Ian Kerridge. Sociol Health Illn 2011
42
21


Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
182
15

Biobanks need publicity.
George Gaskell, Herbert Gottweis. Nature 2011
41
19

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
176
15

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
238
15

Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
137
13

Gift relationships in genetics research.
Richard Tutton. Sci Cult (Lond) 2002
28
25


Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
50
12

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
97
11

Ethical aspects of human biobanks: a systematic review.
Danijela Budimir, Ozren Polasek, Ana Marusić, Ivana Kolcić, Tatijana Zemunik, Vesna Boraska, Ana Jeroncić, Mladen Boban, Harry Campbell, Igor Rudan. Croat Med J 2011
57
11


Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
107
11

Biobanks and the phantom public.
Herbert Gottweis, Haidan Chen, Johannes Starkbaum. Hum Genet 2011
26
23

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
11

Biobank governance in the post-genomic age.
Herbert Gottweis, Georg Lauss. Per Med 2010
19
26

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology.
Paul R Burton, Anna L Hansell, Isabel Fortier, Teri A Manolio, Muin J Khoury, Julian Little, Paul Elliott. Int J Epidemiol 2009
162
9

Tackling community concerns about commercialisation and genetic research: a modest interdisciplinary proposal.
Gillian Haddow, Graeme Laurie, Sarah Cunningham-Burley, Kathryn G Hunter. Soc Sci Med 2007
56
9

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
71
9

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
140
9


Reconsidering the value of consent in biobank research.
Judy Allen, Beverley McNamara. Bioethics 2011
47
10

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
9

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
9

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
9

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
477
9


From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
219
9

Connecting the public with biobank research: reciprocity matters.
Herbert Gottweis, George Gaskell, Johannes Starkbaum. Nat Rev Genet 2011
35
14

Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions.
Daryl Pullman, Holly Etchegary, Katherine Gallagher, Kathleen Hodgkinson, Montgomery Keough, David Morgan, Catherine Street. Genet Med 2012
35
14

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
55
9

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
57
9

Biobanking for Europe.
Martin Yuille, Gert-Jan van Ommen, Christian Bréchot, Anne Cambon-Thomsen, Georges Dagher, Ulf Landegren, Jan-Eric Litton, Markus Pasterk, Leena Peltonen, Mike Taussig,[...]. Brief Bioinform 2008
131
7

Predicting intention to biobank: a national survey.
Christine R Critchley, Dianne Nicol, Margaret F A Otlowski, Mark J A Stranger. Eur J Public Health 2012
46
8


DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
70
7


Biobanks for genomics and genomics for biobanks.
Anne Cambon-Thomsen, Pascal Ducournau, Pierre-Antoine Gourraud, David Pontille. Comp Funct Genomics 2003
27
14

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
42
9

Informed consent in biobank research: a deliberative approach to the debate.
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
83
7

Ethical norms and the international governance of genetic databases and biobanks: findings from an international study.
Alexander Morgan Capron, Alexandre Mauron, Bernice Simone Elger, Andrea Boggio, Agomoni Ganguli-Mitra, Nikola Biller-Andorno. Kennedy Inst Ethics J 2009
28
14


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
138
7

The ethics of biobanking: key issues and controversies.
Heather Widdows, Sean Cordell. Health Care Anal 2011
15
26



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.